Abstract: A surgical system for assisting in the implanting of a glenoid component of a shoulder prosthesis in a patient includes a guide having guide features for guiding application of the bone preparation tool to the glenoid and a series of graphic representations of the glenoid component shown being implanted on the glenoid with different implant positions, each of which is associated with one of the graphic representations.

Abstract: Embodiments of the present invention relate to surgical instrumentation specific to a patient for preparing a bone including a patient-specific block delimiting a supporting surface shaped to fit the bone, and including a main portion partly delimiting the fixed supporting surface and at least two primary orifices for receiving a primary pin, crossing the block between the supporting surface and an opposite surface.

Abstract: A prosthetic assembly and a method of assembling same. The prosthetic assembly includes a base component with at least one engagement surface. A pyrolytic carbon component includes at least one engagement surface. The pyrolytic carbon component is elastically deformed to mechanically interlock with the engagement surface on the base component. The pyrolytic carbon component retains at least a portion of the deformation stress created during coupling with the base component.

Abstract: In order to position an ankle prosthesis including a tibial implant and a talus implant provided with a talo-calcaneal anchoring keel, the invention proposes a surgical instrumentation assembly including: a tibial phantom (60) of the tibial implant, adapted so as to be attached to the tibia (T) of a patient, and an aiming guide (80) adapted for setting into place an instrumentation element (90) through the talus (A) and the calcaneus (C) of the patient, along an axis (Z-Z) for implanting the talo-calcaneal anchoring keel, the tibial phantom and the aiming guide mechanically cooperating with each other to restrict movement of the tibial phantom and the aiming guide relative to each other along vertical and medio-lateral directions, wherein the aiming guide is configured to guide placement of the instrumentation element.

Abstract: Disclosed are products and methods for treating soft tissue injuries. The provided methods include the production of processed or cryopreserved microvascular tissue. Also provided are products and methods of using processed or cryopreserved microvascular tissue for the treatment of soft tissue injuries.

Abstract: This glenoidal component for a shoulder prosthesis comprises a base which may be immobilized on the glenoid cavity of a shoulder, and an element provided to be mounted on this base and forming a convex surface of articulation centred on an axis of symmetry. This axis of symmetry is non perpendicular to a rear face of the base intended to abut against the glenoid cavity, this making it possible to compensate a defect in parallelism between the resectioned surface of the glenoid cavity and the axis of the patient's spinal column. A surgeon can select the component most adapted to the orientation of the resectioned surface from a set of components in which the axes of symmetry of the components are oriented differently with respect to their rear faces.

Abstract: A prosthetic assembly and a method of assembling same. The prosthetic assembly includes a base component with at least one engagement surface. A pyrolytic carbon component includes at least one engagement surface. The pyrolytic carbon component is elastically deformed to mechanically interlock with the engagement surface on the base component. The pyrolytic carbon component retains at least a portion of the deformation stress created during coupling with the base component.

Abstract: This insertion and locking device (1) for an implant in a long bone comprises an elongate body (2) designed to be received in a medullary canal of the long bone, the body defining, in a first position called the insertion position, a first transverse size and, in a second position called the locking position, a second transverse size greater than the first transverse size. This device furthermore comprises drive mechanism (8) suited to enable the body (2) to move from the first position to the second position. In addition, the elongate body (2) comprises a central member (3) defining a main axis and at least one locking member (6) defining at least one axis of movement distinct from the main axis, the or each locking member (6) being suited to anchoring itself in the long bone under the effect of the drive mechanism.

Abstract: A fused loop of an elongated material, such as a surgical suture, and apparatus for making the loop are described. Portions of one or more segments of elongated material may he fused in an ultrasonic welding process to form a welded joint. Multiple materials each with a different melting point may be used for one or more fibers within the elongated material The elongated material may include a sheath, which may be used to protect a core within the elongated material. A fused region of the fused loop may be formed when a material with a lower melting temperature, compared to one or more other materials in the elongated material, is caused to melt. A related ultrasonic welding apparatus may include a temperature sensor for control of the welding process.

Abstract: A humeral head augment device for use in a modular shoulder prosthesis. The humeral head augment device has an external bearing surface with at least one surface portion that includes a radius of curvature. The radius of curvature is configured to constrain translational movement of the implanted shoulder prosthesis when the humeral head augment device is positioned within the shoulder prosthesis. The humeral head augment device also includes a coupling mechanism designed to lock the humeral head augment device to either the stem or the humeral head, thereby ensuring proper operational positioning of the device within the shoulder prosthesis and allowing the implanted shoulder prosthesis to function in a patient suffering from rotator cuff arthropathy. A shoulder prosthesis using a humeral head augment device, a method for assembling a shoulder prosthesis and method for using a humeral head augment device in a shoulder prosthesis are also disclosed.

Abstract: This glenoidal component for a shoulder prosthesis comprises a base which may be immobilized on the glenoid cavity of a shoulder, and an element provided to be mounted on this base and forming a convex surface of articulation centered on an axis of symmetry. This axis of symmetry is non-perpendicular to a rear face of the base intended to abut against the glenoid cavity, this making it possible to compensate a defect in parallelism between the resectioned surface of the glenoid cavity and the axis of the patient's spinal column. A surgeon can select the component most adapted to the orientation of the resectioned surface from a set of components in which the axes of symmetry of the components are oriented differently with respect to their rear faces.

Abstract: An instrument is disclosed including: a top jaw member extending between a proximal end and a distal end and including a first top anchor target slot and a second top anchor target slot; a bottom jaw member extending between a proximal end and a distal end and including a first bottom anchor target slot and a second bottom anchor target slot; and a joint member connected to the proximal ends of the top jaw member and the bottom jaw member.

Abstract: This surgical apparatus comprises, on the one hand, means for spatial marking-out of the kneecap and femur of a patient to be operated on, and, on the other hand, means for simultaneous and relative representation of this kneecap provided virtually with a patellar implant of the prosthesis, and of this femur provided virtually with a femoral implant of the prosthesis, in a sagittal plane passing both through the kneecap and through the trochlea of the aforementioned femoral implant. Using this apparatus, the surgeon can easily and quickly check the antero-posterior size of the prosthesis in order to reduce the risks of subsequent dislocations of the kneecap fitted with the prosthesis.

Abstract: A prosthesis and method for a ball and socket joint. The prosthesis includes a first component including an anchoring shank and a metaphyseal portion. The metaphyseal portion includes a first articular surface configured to move in translation relative to the anchoring shank. An intermediate component includes a first articular surface configured to engage with the first articular surface on the metaphyseal portion, and a second articular surface configured to engage with the ball and socket joint.

Abstract: The aim of the invention is to restore the mobility of an articular end (2) of a bone (3) of a patient by means of a reconstruction implant. This implant (1), which permits reconstruction both of bone and of cartilage, comprises a grated framework (10) and a sheet (20) made of a biological tissue material, this sheet firmly covering one face (11) of the framework, while the opposite face (12) is designed to be pressed rigidly against, and firmly joined to, the end of the bone.

Abstract: A bone staple (10) for securing a first bone region (12A) to a second bone region (12B) includes a staple body (16) having a first leg section (18), a second leg section (20), and a connector section (22). The first leg section (18) is insertable into the first bone region (12A). The second leg section (20) is insertable into the second bone region (12B). The connector section (22) connects the first leg section (18) to the second leg section (20). The connector section (22) includes a deformable region (22A) that is movable from a first configuration (14A) in which the leg sections (18) (20) are spaced apart a first distance (24) and a second configuration (14B) in which the leg sections (18) (20) are spaced apart a second distance (26) that is less than the first distance (24). In one embodiment, compression of the deformable region (22A) causes the deformable region (22A) to move from the first configuration (14A) to the second configuration (14B).

Abstract: A humeral head augment device for use in a modular shoulder prosthesis. The humeral head augment device has an external bearing surface with at least one surface portion that includes a radius of curvature. The radius of curvature is configured to constrain translational movement of the implanted shoulder prosthesis when the humeral head augment device is positioned within the shoulder prosthesis. The humeral head augment device also includes a coupling mechanism designed to lock the humeral head augment device to either the stem or the humeral head, thereby ensuring proper operational positioning of the device within the shoulder prosthesis and allowing the implanted shoulder prosthesis to function in a patient suffering from rotator cuff arthropathy. A shoulder prosthesis using a humeral head augment device, a method for assembling a shoulder prosthesis and method for using a humeral head augment device in a shoulder prosthesis are also disclosed.

Abstract: A surgical instrument including at least one tibial phantom generally corresponding to at least certain features of the tibial implant. The tibial phantom includes a top surface adapted to move freely against the prepared bottom end of the tibia. At least one talus phantom generally corresponding to at least certain features of the talus implant is engaged with the prepared top surface of the talus. At least one phantom skid is located between the tibial phantom and the talus phantom. The phantom skid is engaged with the tibial phantom such that dynamic engagement between the phantom skid and the talus phantom through at least extension and flexion of the ankle joint positions the tibial phantom on the prepared bottom end of the tibia. The phantom skid can either be a part of the tibial phantom or a separate component.

Abstract: A fused loop of an elongated material, such as a surgical suture, and apparatus for making the loop. Portions of one or more segments to be joined together are fused in a welding process to form a welded joint. The shear area of the fused portion of the joint determines the strength of the joint and is thus preferably relatively large. Various configurations for the welding apparatus facilitate the creation of relatively large fused portions of the joint by maximizing contact between at least one of the welding members of the apparatus and at least one of the segments to be joined.